Female reproductive parameters in the Javan gibbon (Hylobates moloch)

Javan gibbons (Hylobates moloch) are one of the most endangered gibbon species in the world. Data on the reproductive biology of the species are almost nonexistent, and a general understanding of the female reproductive biology of this species is important for both ex situ and in situ conservation. Using 18 years of data from 11 captive individuals, we provide new information on the reproductive biology of Javan gibbons based on sexual swelling and menstrual bleeding, including reproductive development, interbirth intervals, and ovarian cycle lengths. Menarche and the onset of sexual swelling occurred at 6.2 and 6.5 years respectively, followed by a period of adolescent sterility of about 1.5 years. Average age at first birth was 8.8 years, and interbirth intervals were about 2.3 years, decreasing to 1.0 year during cases of infant mortality at or shortly after birth. Ovarian cyclicity was measured through periods between menstrual bleeding and sexual swelling. Menstrual bleeding indicates the start of a new ovarian cycle, while sexual swelling normally occurs near the time of ovulation. Menstrual bleeding intervals gave a cycle length of 25.6 days, while sexual swelling intervals gave a cycle length of 27.3 days. These both correspond closely to cycle lengths in other gibbon species, as well as hormonal studies in Javan gibbons. In particular, observing the presence/absence of swellings was found to be a useful and easy method to monitor female ovarian cycles, and could be a practical noninvasive technique for caretakers and researchers. Zoo Biol 29:449–456, 2010. © 2009 Wiley‐Liss, Inc.     

Reproductive biology of captive and free-ranging spider monkeys

Records from 42 zoos and from long-term studies of wild populations were analysed to describe the reproductive biology of spider monkeys (Ateles spp.). Both data sets suggested that spider monkey females typically have their first infant between 7 and 8 years of age with an interbirth interval of approximately 32–36 months. Infant sex ratio for zoo populations was approximately 1 male to 1 female; infant sex ratios from wild populations were variable. Zoo records provided adequate sample size to suggest that interbirth interval was not influenced by the sex of the infant produced, and that the sex ratio and the probability of infant survival did not change with the number of infants the mother had produced. The findings of this study have implications with respect to the conservation of New World primate species. Since spider monkeys take a long time to reach sexual maturity and their interbirth interval is longer than that expected based on their body size, their populations may be slow to recover following disturbances. Thus, particular care should be taken for the protection of these species.     

Some reproductive parameters of stumptailed macaques (Macaca arctoides)

Reproductive records kept from 1969 to 1981 were used to study menstrual cycles, pregnancies and births of eight colony-housed stumptailed macaques. The findings for annual distribution of births, pregnancy duration and infant sex ratio were consistent with previous reports. The interbirth interval after infant loss was significantly shortened from the interbirth interval when infants were maintained with their mothers. Vaginal bleeding during early lactation indicates that stumptails are not necessarily characterized by a prolonged period of postpartum amenorrhea. Complete copulation was observed prior to six months postpartum, but interbirth intervals indicate that conception did not occur prior to that time. Interbirth intervals tended to be shorter for dominant than for subordinate females and to lengthen as a function of increasing age.     

Birth intervals ofCercopithecus monkeys of the kakamega forest,Kenya

Data on interbirth intervals are reported for two forest-living guenons,Cercopithecus mitis andC. ascanius, from a western Kenyan site. Measured intervals for females whose first offspring survived varied from 24 to 54 months (median 47,N=10) forC. mitis, and from 49 to 60 months (median 52,N=3) forC. ascanius. Intervals were shorter when the first of two offspring died. These results are supported by data on estimated intervals, in which the date of the first of two births was estimated, and incomplete intervals. Our measurements exceed previous estimates of interbirth intervals in wild populations and measured intervals of captive animals. Compared to closely related species inhabiting unpredictable and seasonal environments, these forest guenons breed very slowly indeed.     

Impact of Male Takeovers on Infant Deaths,Births and Conceptions in Cebus capucinus at Santa Rosa,Costa Rica

Male takeovers are associated with infant wounding and death in 3 of 4 capuchin species. In this paper, I analyze the effects of male takeovers on infant mortality and the subsequent conceptions and interbirth intervals of their mothers over an 18-yr period and test predictions of the sexual selection model of infanticide for white-faced capuchins, (Cebus capucinus). Major findings are that infants are significantly more likely to die in the 3- and 12-mo periods following a takeover than in times of peace and that a female whose infant dies experiences a significantly shorter interbirth interval before her next infant is born than she would have had the former infant survived. In the vast majority of cases, the invading males become resident in the group and are present during the subsequent conceptions of the females in the group. However, overall conception rates do not rise significantly in the year after a takeover, there is no relationship between the age of the infant at death and the length of the mother's subsequent interbirth interval, and it is not yet clear if male infants are preferentially targeted by invading males. Most takeovers occur during the 6-mo dry season and most conceptions occur in the wet season, 3–6 mo later. My findings support the major predictions of the sexual selection model of infanticide in primates and demonstrate that male takeovers of social groups have substantial effects on infant survival and maternal parturition patterns in Cebus capucinus.     

Interbirth interval variation in three sympatric species of neotropical monkey

Relatively few papers have focused on interbirth intervals in primates, even though the spacing between births is one of the primary determinants of female reproductive success in long-lived mammals. We present life history data from a ten-year field study of Costa Rican capuchins (Cebus capucinus), howlers (Alouatta palliata), and spidei monkeys (Ateles geoffroyi). Analyses of intraspecific variability found no significant differences attributable to individual variation in age, parity, weight, or maternal rank. Loss of an infant significantly shortened the interbirth interval in all three species. There was no correlation between annual rainfall and birth rates, but there was a significant clustering of births in the dry season. Survival analyses demonstrated a significant difference between the median interbirth intervals of the three species. Howlers have the shortest intervals (19.9 months), capuchins exhibit longer intervals (26.36 months), and spider monkeys have the longest intervals (34.72 months;. This comparative pattern does not correspond to relative body weights of the three species, but does correspond to relative brain weights. Comparisons to other primates with similar life history characteristics demonstrate that interbirth intervals are best examined at the level of their three component phases: gestation, lactation, and cycling to re-conception. © 1995 Wiley-Liss, Inc.     

Estimating hominid life history: the critical interbirth interval

Unlike any great apes, humans have expanded into a wide variety of habitats during the course of evolution, beginning with the transition by australopithecines from forest to savanna habitation. Novel environments are likely to have imposed hominids a demographic challenge due to such factors as higher predation risk and scarcer food resources. In fact, recent studies have found a paucity of older relative to younger adults in hominid fossil remains, indicating considerably high adult mortality in australopithecines, early Homo, and Neanderthals. It is not clear to date why only human ancestors among all hominoid species could survive in these harsh environments. In this paper, we explore the possibility that hominids had shorter interbirth intervals to enhance fertility than the extant apes. To infer interbirth intervals in fossil hominids, we introduce the notion of the critical interbirth interval, or the threshold length of birth spacing above which a population is expected to go to extinction. We develop a new method to obtain the critical interbirth intervals of hominids based on the observed ratios of older adults to all adults in fossil samples. Our analysis suggests that the critical interbirth intervals of australopithecines, early Homo, and Neanderthals are significantly shorter than the observed interbirth intervals of extant great apes. We also discuss possible factors that may have caused the evolutionary divergence of hominid life history traits from those of great apes.     

Reproductive parameters of mandrills at the Tulsa Zoo

The genital swelling patterns and birth records of female mandrills housed at the Tulsa Zoo between 1979 and 1992 were examined to determine various reproductive parameters. Mean age at first adolescent genital swelling was 2.7 years (sd = .55), first adult swelling was 3.7 years (sd = .64), and first conception was 5.1 years (sd = 1.30). Genital swelling cycle duration averaged 39.6 days (n = 33 cycles), with the swelling phase averaging 19.5 days (n = 51 cycles). There was no interindividual difference in cycle length (F = 1.26, P = .31) or swelling duration (F = 0.65, P = .58), nor was there a difference in cycle length (F = 0.47, P = .50) or swelling duration (F = 1.27, P = .27) before and after first parturition. Duration of gestation was estimated to be 165.9 days (sd = 3.3; n = 17 pregnancies). Lactational anestrus averaged 10.1 months, whereas mean interbirth interval was 17.9 months (n = 11). There was a significant negative correlation between age of the mother and interbirth interval (r = ?;0.648, P = .03). Data presented in this report provide a comprehensive profile of reproductive parameters for zoo-housed mandrills, which may aid other facilities in the reproductive management of their captive groups. © 1995 Wiley-Liss, Inc.     

Determinants of fecundity and reproductive success in captive vervet monkeys

Between 1975 and 1983, adult female vervet monkeys (Cercopithecus aethiops sabaeus) over 3.5 years of age, living in two undisturbed social groups in a captive colony in Sepulveda, California, have averaged 1.0 births per female year with a mean interbirth interval of 10.7 months. Increased fecundity did not result in decreased survival rates of offspring in this population. Fecundity was influenced by the mother's age and dominance rank. The primary factor in the age-fecundity relationship was the age at first birth, which varied from three to five years. High-ranking females contributed the most to the high rate of fecundity, with significantly shorter interbirth intervals, more births per female year, and more surviving infants compared to low-ranking females.     

Lactation and interbirth interval in the Senegal galago (Galago senegalensis moholi)

Five years of reproductive data on Galago senegalensis moholi at the Duke University Primate Center were examined to determine the effect of lactation on interbirth interval and its component phases, postpartum anovulatory interval and interval from onset of estrous cycles to conception. Females whose infants died within 3 weeks of birth had significantly shorter interbirth intervals and postpartum anovulatory intervals than did females who raised their infants until weaning.     

Troop history,female reproductive strategies and timing of male change in Hanuman langurs,Presbytis entellus

Female reproductive data are presented from 9 years of longitudinal observations on two troops of Hanuman langurs (Presbytis entellus) living around Jodhpur, India. On the basis of 89 live births interbirth intervals were calculated to examine the effect of demographic factors on reproductive behaviour and troop composition. Sex of an infant seems to influence the length of intervals which are longer after the birth of female infants at an average of 1.7 months. It is suggested that this may be an outcome of differential maternal investment by allocating more time and energy towards female infants who run a higher mortality risk than male infants, at least up to an age of 27 months. Troopspecific interbirth intervals are influenced by social events. If the last infant is still alive when the next one is conceived, the intervals are significantly longer than after the premature loss of an infant (Bijolai troop: 15.6 vs. 12.1 months; Kailana-1 troop: 16.7 vs. 11.4 months). During undisturbed male tenureship intervals are shorter than after a male change (Bijolai troop: 14.3 vs. 16.0 months; Kailana-I troop: 15.6 vs. 17.5 months). Thus the frequency of male changes can influence the demography of a troop. Furthermore, the data suggest that take-overs are optimally timed by males. New males tend to take over a troop when most of the females are cycling.     

Sexual behavior and reproduction ofCercocebus albigena johnstonii in Kibale forest,Western Uganda

Gray-cheeked mangabeys live in multimale social groups. Two groups of these monkeys were studied extensively over a period of 22 months, and a further eight groups were observed opportunistically. Data on the occurrence of sexual swelling infernales were collected and the different phases of swelling and deflation are described in detail together with data on their duration. The data were found to agree broadly with those presented by other workers on captive animals. Pre and postpartum swellings are described. The majority of copulations was observed to occur at peak swelling and a specific gesture, the head flag, was noted as a solicitation. The data on initiation of copulations show that the males initiated more copulations than the females. However, female-initiated copulations ended in ejaculation more often than male-initiated copulations. The behaviors of the mangabeys during precopulation and copulation were found to be broadly similar to those of the macaque. Copulations were observed most often on the day of peak swelling;however, adult males were the only animals to copulate prior to peak swelling. Subadult male copulations were most often after peak swelling. Masturbation was observed to ejaculation on two occasions. The data show gestation periods of between 184 and 189 days. A mean interbirth interval was calculated to be 33.33 ± 15.87 months.     

Reproduction in wild female olive baboons

The purpose of this paper is to evaluate several factors that influence female reproduction in a large troop of wild olive baboons (Papio cynocephalus anubis) based on 4 consecutive years of demographic data. Interbirth intervals were significantly shorter for females whose infants died before their next conception than for females whose infants survived. High-ranking mothers of surviving infants had significantly shorter birth intervals than comparable low-ranking mothers, independent of maternal age. This occurred mainly because the interval from resumption of cycling to conception was significantly shorter for high-vs. low-ranking females. Dominance rank did not influence sex ratio at birth, infant survival in the first 2 years, or adult female mortality. Age was also significantly related to interbirth intervals, with older females having shorter intervals. Primiparous females had consistently longer reproductive intervals than did multiparous females, but this difference reached statistical significance only for females whose infants died before the next conception. Primiparous females also experienced significantly higher infant mortality. Data on body size and estrous cycle length indicated no differences between high- and low-ranking females. Nutritional and stress-related mechanisms that may underlie the reproductive advantages of high rank are discussed.     

Development of ecological competence in Sumatran orangutans

Data on orangutans (Pongo pygmaeus abelii) living in a Sumatran swamp forest yield an estimated median interbirth interval of at least 8 years, concurring with findings from other sites. This longest known mammalian interbirth interval appears due to maternal amenorrhea during the long exclusive dependence of the offspring. We describe the development of various components of offspring independence. In this arboreal ape, 3‐year‐olds had largely reached locomotor independence. Nest‐building skills were also well‐developed in 3‐year‐olds, but immatures shared their mother's nest until weaned at around age 7. At time of birth of the new sibling, association with the mother had begun to decline for both male and female offspring, suggesting that the immatures had mastered all the necessary skills, including basic tool use, to feed themselves. By about 11 years of age, they also ranged independently from the mother. These results show that orangutans do not develop independence more slowly than chimpanzees. Why, then, is weaning 2 years later in orangutans? In chimpanzees, mothers are often accompanied by two or even three consecutive offspring, unlike in orangutans. This contrast suggests that an orangutan mother cannot give birth until the previous offspring is ecologically competent enough to begin to range independently of her, probably due to the high energy costs of association. Thus, the exceptionally long interbirth intervals of orangutans may be a consequence of their solitary lifestyle. Am J Phys Anthropol, 2004. © 2004 Wiley‐Liss, Inc.     

Birth spacing in langur monkeys (Presbytis entellus)

This paper presents 10 years of reproductive data on birth interval length and 5 years of data on reproductive behavior postpartum from a captive colony of gray langur monkeys (Presbytis entellus)housed in Berkeley, California. Birth intervals of females following different pregnancy and nursing schedules are compared. Females whose infants survive to the age of 9 months have a median birth interval of 15.4 months. The experimental separation of mothers from infants for a period of 2 weeks, 6 to 9 months postpartum, had no significant effect on the median birth interval length. Females experiencing a pregnancy failure or the loss of a neonate had median birth intervals of 9.6 and 10.7 months, respectively. These intervals were significantly shorter than the birth intervals of females whose infants survived to 9 months, showing that the presence of a nursing infant delays the female’s time to next conception by approximately 5 to 6 months. Females experienced a median of three estrous periods (two estrous cycles) before conceiving postpartum, regardless of pregnancy outcome or length of infant survival, and females rarely conceived during their first estrous period postpartum. Weaning did not occur until after the mother’s next conception. These data indicate that, in populations of langurs characterized by average birth intervals of 15 to 16 months, the loss of an infant after the age of 5 to 6 months will not accelerate a female’s ability to conceive or shorten the birth interval length. The available data on birth spacing from populations of free-ranging langurs are reviewed. It could not be demonstrated that non-Himalayan populations are characterized by birth intervals which are as long as 20 to 24 months. Rather, it is suggested that female langurs inhabiting seasonally arid sites, such as Jodhpur, Abu, and Dharwar, may be capable of producing infants on the average of every 15 to 16 months. Flexibility in the timing of births and the lack of well-defined birth seasons at these sites may be explained by this species’ dietary and digestive adaptations. Additionally, data on birth spacing and the age of missing infants from the above field sites, where it has been suggested that infanticide following changes in male leadership occurs habitually, do not lend support to the sexual selection hypothesis of infanticide as proposed by S. Hrdy (1974, 1977).     

Reproduction in the slender loris (Loris tardigradus malabaricus)

A breeding colony of slender lorises (Loris tardigradus malabaricus) was studied to obtain data for comparison with other prosimian species, to contribute reproductive information for improving management of captive lorises, and to resolve some uncertainties in the literature regarding reproduction in the slender loris. At the Duke University Primate Center, a female slender loris reached sexual maturity at approximately ten months of age and conceived at one year of age. The length of the estrous cycle was 29–40 days, with copulation occurring over two consecutive days during estrus. Gestation length was 166–169 days. Litter size for each six births was one. Conception did not occur during an immediate post-partum estrus, but four months after birth, resulting in a 9 1/2-month interbirth interval. There was no evidence of reproductive seasonality. Lactation lasted between five and seven months. Reproductive rates of slender lorises are among the lowest of primates less than 500 g. Differences in reproductive parameters may exist between different subspecies of slender lorises.     

Longitudinal patterns of reproduction in wild female siamang (Hylobates syndactylus) and white-handed gibbons (Hylobates lar)

I present the 6- year reproductive histories of three wild female siamang (Hylobates syndactylus)and four white-handed gibbons (Hylobates lar)at the Ketambe Research Station (Sumatra, Indonesia). Reproductive output varied considerably among females. Two females failed to gestate: both were nulliparous young adult H. lar,one of which remained unpaired for 4 years after dispersing from her group, while the other lost her recently acquired mate to another female. Only one- (a white-handed gibbon)- gave birth more than once, yielding interbirth intervals of 22 and 31 months. Pair bond stability or reduced interspecific feeding competition or both factors may have contributed to the brevity of these intervals. The other females- one H. lar,and three H. syndactylus-each gave birth once, suggesting minimum interbirth intervals exceeding 4–5 years (H. lar)and 3 years (H. syndactylus)in these individuals. Even given the pronounced variation observed among H. lar,these data suggest that interbirth intervals may often exceed the 2- to 3- year interval commonly attributed to these two species. Sources of reproductive failure were 1) maternal abandonment of the neonate due to impaired ability to provide maternal care (H. syndactylus,),(2) premature or stillbirth (H. syndactylus,),and (3) pregnancy termination (H. lar).These data and a review of information on longevity and age at menarche suggest that the actual lifetime reproductive output of a siamang or white-handed gibbon female may often fall far short of the 10 offspring/lifetime originally proposed for these species. Indeed, females may rear as few as five offspring to weaning in a lifetime, which is a figure reminiscent of the reproductive potential of some pongids. Finally, variance in female reproductive success is higher than expected in these monogamous species, which suggests that females (and males) are under strong selective pressure to exert mate choice, possibly through acquisition of (new) mates and extrapair copulations. Future research must clarify the availability of opportunities for paired adults to engage in these sociosexual behaviors.     

Birth dynamics in Hanuman langurs,Presbytis entellus of Jodhpur,India

Ten years data on birth peak, birth rate and interbiith interval inPresbytis entellus of Jodhpur have been presented. Although Hangman langur females breed round the year, there is some concentration of births during January–March while fewer births occur during October–December. It seems that provisioning and crop raiding together may provide better feeding opportunities to breed year round. However, it remains unclear whether environmental factors allow langur females to deliver more infants during January–March. During 1984–86 the birth rate was uniform for the whole population (0.63). While there was a variation within the troops from year to year, data suggest that resident male replacements do alter birth rate. It goes down when resident males are replaced frequently. The interbirth interval ranges between 7.0 and 76.5 months (average, 16.88 months;n = 112). Abortions and still-births reduced the interbirlh interval to 7.1 months (range 7.1-21.1; average, 11.4 months;n= 8) compared to the normal inlerbirth interval following infant survive its first 4.1 months of life (range 10.7-76.5 months; average, 17.28 months;n = 86). However, infant loss under the age of 4.1 months did not reduce the interbirth interval except in two cases (range 7.0-51.8 months; average, 17.27 months;n = 18). Maternal rejection or weaning begins at about 8 months of age and lasts until infants are 12 months old. In this population, the probability of twin births was worked out to be 0.79 per 100 births.     

Life-history characteristics of a wild population of vervets (Cercopithecus aethiops sabaeus) in Barbados,West Indies

Life history data are presented for a population of vervets, Cercopithecusaethiops sabaeus, in Barbados, West Indies. The data were obtained from two habituated troops and from vervets captured during a large-scale trapping program. Individuals of known age from one troop were weighed periodically, and separate growth curves generated for males and females. The mean weight of captured adult females was 3.3 kg; that of adult males, 5.3 kg. The average age at sexual maturity is estimated at 34 months for females and 60 months for males. Vervets give birth throughout the year, but most infants are born between April and July. The average interbirth interval following a surviving infant is 11.8 months. The mortality of juveniles is heaviest between birth and 2 years of age and decreases thereafter. Males emigrate from their natal troops at sexual maturity and one incident of a juvenile female emigrating is reported.